# FDA Inspection 1260826 - KinOmega Biopharm Inc. - January 24, 2025

Source: https://www.globalkeysolutions.net/records/fda_inspections/kinomega-biopharm-inc/dbac81cd-866b-4a75-8edf-51861c217ed9
Source feed: FDA_Inspections

> FDA Inspection 1260826 for KinOmega Biopharm Inc. on January 24, 2025. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1260826
- Company Name: KinOmega Biopharm Inc.
- Inspection Date: 2025-01-24
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Drug Quality Assurance
- Product Type: Drugs
- Office Name: Center for Drug Evaluation and Research

## Related Documents

- [FDA Inspection 1260826 - 2025-01-24](https://www.globalkeysolutions.net/records/fda_inspections/kinomega-biopharm-inc/18634cbc-7121-49e0-bfdd-4d799653b125)

Company: https://www.globalkeysolutions.net/companies/kinomega-biopharm-inc/f841a0a7-9711-4f02-8333-be77a1eab703

Office: https://www.globalkeysolutions.net/offices/center-for-drug-evaluation-and-research/cd980d74-1cbf-4226-ba9a-9045324c236c